HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → ethyl 2-acetyl-6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-9-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18328986 | HCID 18328986 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-acetyl-6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-9-carboxylate | HCID 18794216 | 70% |
Reaction Steps
Sodium hydroxide (3 g), tetrabutylammonium hydrogen sulphate (1.87 g) and ethyl chloroformate (2.2 mL) are successively added to a solution of 1-(6-methoxy- 1-methyl-2,3,4,9-tetrahydro-1H-β-carbolin-2-yl)-1-ethanone (1.45 g) in dichloromethane (100 mL). The mixture is stirred at room temperature for 3 h. After separation on silica gel (chloroform/methanol eluent), the ethyl 2-acetyl-6-methoxy-1 -methyl-2,3,4,9-tetrahydro-1H-β-carboline-9-carboxylate is obtained (70% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048868 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-0e949290e988481d916e0685d660a6f3 |
| Source note | uspto-grants-2000_04 |